Inhalt
Documenting medical devices has some significant differences from documenting business software or industrial machinery. Regulatory issues create unique demands on the TC that are not always logical or intuitive.
In this session, learn the key differences between generic TC content and content for medical devices.
Das lernen Sie
- understand how the project life-cycle differs from software
- learn to work with regulatory SMEs
- balance the needs of the user with regulatory demands
- …and more
Vorkenntnisse
General product documentation experience
Referent:in
Leah Guren
- Cow TC
- Zum Profil
Biografie